Page 102 - Tunable Lasers Handbook
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4  CO,  Isotope Lasers and Their Applications   83

                    (v = v,),  a narrowband resonant dip appears in the intensity of  the laser output
                    power,  because  the  traveling-wave  components constituting the  standing-wave
                    field interact with  the same group of  molecules (or atoms). namely, those that
                    have zero velocity in the direction of the laser's optical axis (k.is=O).  This dip in
                    the laser's output power was first verified by  Szoke and Javan in the output of a
                    He-Ne  laser  at  1.15 pm  [66]. and was appropriately named "Lamb-dip"  since
                    Lamb predicted its occurrence.
                        An even more useful variant of the standing-wave saturation resonance was
                    first  demonstrated  by  Lee  and  Skolnick  [67]  who  inserted  a  low-pressure
                    absorber gas cell, which had a resonantly interacting absorption line, within the
                    standing-wave field of the laser's optical cavity. In this case the narrow resonant
                    change appeared as a "pip"  increase in the laser's output power and was named
                    "inverted Lamb-dip."
                        To  a very  good first approximation. the line shapes and FWHM widths of
                    the Lamb-dips and the inverted Lamb-dips are determined by collision broaden-
                    ing and thus have Lorentzian profiles. In actual practice the absorber gas refer-
                    ence cells can be  effectively used  with much lower pressure gas fills than the
                    typical mixture pressures required to operate gas lasers. Thus both  in principle
                    and  in  practice  the  long-term  frequency  stabilization techniques  utilizing  the
                    inverted Lamb-dip can provide much better frequency discriminators than those
                    using the Lamb-dip.
                        One of the best known early examples of inverted Lamb-dip stabilization is the
                    methane-(CH,)  stabilized He-Ne  laser oscillating at 3.39 pm. This absorber-laser
                    combination was  first suggested and demonstrated by  Shimoda in  1968 [68] and
                    was also extensively studied and utilized by Barger and Hall [69].
                        In the case of the CO, laser system the initial attempts to use CO, itself as a
                    reference via either the Lamb-dip or the inverted Lamb-dip techniques were not
                    very  successful. Lamb-dip was  only  obtained with  very  low-pressure laser gas
                    fills and  was  prone to  severe asymmetrical distortions due to competition from
                    adjacent transitions [70]. The inverted Lamb-dip stabilization method on the other
                    hand required very long (-1.7-m)  CO,  absorption cells heated to several hundred
                    (400°C) degrees above room temperature [71]. The poor results were due to the
                    fact that the lower state rotational-vibrational levels of  the CO,  laser transitions
                    do not belong to the ground state. and therefore the absorption coefficient of low-
                    pressure room-temperature CO,  at  10 ym  is very  small. The  small absorption
                    coefficient in  turn  made  it  difficult to  observe  and utilize directly the  inverted
                    Lamb-dip resonance in the full-power output of  the CO, laser. These difficulties
                    were overcome at Lincoln Laboratory in  1970, when. atthe suggestion of Javan.
                    we (Freed and Javan) first demonstrated [18] that excellent long-term frequenc?
                    stability and reproducibility of  CO,  lasers can be readily  obtained (and greatly
                    improved on if necessary) by the frequency stabilization of the lasers to the srand-
                    ing-wave saturation resonance observed in the 1.3-ym upper-state-to-ground-state
                    fluorescence of CO,.  as graphically illustrated in Fig. 8.
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